Job summary
Job post source
This job is directly from Tandem Clinical Research
Job overview
The Clinical Research Assistant role at Tandem Clinical Research supports clinical trials by assisting in study coordination, patient interaction, and data collection to ensure protocol adherence and trial success.
Responsibilities and impact
The assistant will understand study protocols, collect and process samples, interview patients, assist coordinators, perform clinical tasks like phlebotomy and ECG, maintain documentation, educate patients, and support community outreach.
Compensation and benefits
The position offers a starting salary of $40,000 per year with benefits including 401(k), dental, health, and vision insurance, and paid time off.
Experience and skills
Candidates should have proficiency in Microsoft Office, preferably knowledge of EMR systems, and good communication and organizational skills; Spanish and prior clinical trial or healthcare experience are advantageous.
Company information
Tandem Clinical Research is dedicated to testing investigational medications and devices across various diseases and disorders.
Job location and travel
The job is located in Viera, FL, requiring relocation before starting, with work performed in person during an 8-hour shift.
Company overview
Tandem Clinical Research is a company that specializes in conducting clinical trials and research studies, primarily focusing on advancing medical science and improving patient care. They generate revenue by partnering with pharmaceutical companies, biotechnology firms, and medical device manufacturers to conduct trials that test the safety and efficacy of new treatments and therapies. Founded with a commitment to innovation and quality, Tandem Clinical Research has built a reputation for its rigorous approach to clinical trial management and its ability to deliver reliable and timely results. The company is known for its collaborative work environment and dedication to ethical research practices, making it an attractive employer for those passionate about contributing to medical advancements.
How to land this job
Tailor your resume to highlight your experience with clinical trial protocols, patient interviews, and specimen handling to align with the Clinical Research Assistant role at Tandem Clinical Research.
Emphasize skills in communication, organization, and proficiency with Microsoft Office, as well as any experience with EMR systems or clinical trials, to match the job requirements.
Apply through multiple channels including Tandem Clinical Research's corporate career site and LinkedIn to maximize your application visibility.
Connect with current employees in the clinical research or study coordination teams at Tandem Clinical Research on LinkedIn; initiate conversations by commenting on recent company projects or asking about team culture and study management practices.
Optimize your resume for ATS by incorporating keywords such as 'clinical trial protocols,' 'patient interviewing,' 'specimen processing,' 'EMR systems,' and 'clinical research coordination' to ensure it passes automated screenings.
Use Jennie Johnson's Power Apply feature to automate submitting tailored applications across multiple platforms and identify LinkedIn connections for networking, freeing up your time to prepare for interviews and further research.
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